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Peter Juma Ochieng, Zoltán Maróti, József Dombi, Miklós Krész, József Békési and Tibor Kalmár
Copy number variation (CNV) is a form of structural variation in the human genome that provides medical insight into complex human diseases; while whole-genome sequencing is becoming more affordable, whole-exome sequencing (WES) remains an important tool...
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